| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92784932-92785184 | Common:3; Rare:97 | ||||
| chr1:92831972-92832133 | Common:1; Rare:84; Clinvar:7; Clinvar (benign):7 | ||||
| chr1:92961427-92961826 | Common:3; Rare:121 | ||||
| chr1:93079111-93079308 | Common:2; Rare:81 | ||||
| chr1:93179867-93179970 | Common:1; Rare:28 | ||||
| chr1:93180043-93180738 | Common:1; Rare:271 | ||||
| chr1:93345676-93345962 | Common:5; Rare:101 | ||||
| chr1:93447985-93448257 | Common:3; Rare:85 | ||||
| chr1:93847190-93847273 | Common:1; Rare:24 | ||||
| chr1:93879083-93879274 | Common:1; Rare:73 | ||||
| chr1:93909568-93909632 | Common:1; Rare:22 | ||||
| chr1:94237435-94237737 | Rare:110 | ||||
| chr1:94418303-94418490 | Common:2; Rare:76 | ||||
| chr1:94541633-94542001 | Common:1; Rare:106 | ||||
| chr1:94820151-94820557 | Common:6; Rare:109 |